Clinical Research Assistant I
Children's Hospital of Philadelphia • Philadelphia, PA2d • Onsite
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Clinical Research Assistant I
Children's Hospital of Philadelphia•Philadelphia, PA
•Onsite
About The Position
The Clinical Research Assistant I will join the research team of Dr. Alexander Fiks, Dr. Brian Jenssen and Dr. Stephanie Mayne at Clinical Futures and PolicyLab at The Children’s Hospital of Philadelphia. The open position will involve work in these and related areas with a particular concentration on supporting a trial focused on parent/caregiver tobacco treatment and innovation in clinical care delivery. The candidate will also join the Possibilities Project, an initiative focused on transforming pediatric primary care to improve care delivery and child/family health and wellness. The team values a growth mindset and shares a commitment to lifelong learning and fostering career development among team members. Under the direct supervision of the Principal Investigator and/or other study team members, this role provides support in the conduct of clinical research. Job responsibilities may include human subject research activities including but not limited to subject enrollment, data/sample collection, data entry, and regulatory submissions support.
Requirements
- High School Diploma / GED Required
- Previous relevant clinical research experience Required
- At least one (1) year of relevant clinical research experience
- Familiarity with IRB and human subject protection.
Nice To Haves
- Bachelor's Degree Preferred
Responsibilities
- Provide technical and administrative support in the conduct of clinical research: Patient/research participant scheduling
- Patient/Research Participant screening for inclusion/exclusion criteria or case history
- Data collection
- Data entry
- Data management
- Laboratory sample processing
- Clinical research study procedures or questionnaire administration
- Organization of research records and/or other study related documentation
- Research Study Compliance
- Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
- Comply with Institutional policies, SOPs and guidelines
- Comply with federal, state, and sponsor policies
- Consent subjects, with appropriate authorization and training
- Document and report adverse events
- Maintain study source documents
- Complete case report forms (paper and electronic data capture)
- Assist with IRB/regulatory submissions
- Complete case report forms or other study documentation (paper and electronic data capture)
- Follow-up care
- Order materials/supplies
- Schedule research meetings
Benefits
- Annual influenza vaccine
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
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